A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638537



Internal ID7025322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46629829..46654810hg38UCSC Ensembl
chr16:46663741..46688722hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3824982
hg1924982
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15471944
SamplesHG01841
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638537
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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